HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159322663T>A , CM000667.2:g.159322663T>A | GRCh38 |
NC_000005.9:g.158749671T>A , CM000667.1:g.158749671T>A | GRCh37 |
NC_000005.8:g.158682249T>A | NCBI36 |
NG_009618.1:g.12811A>T , LRG_71:g.12811A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-148-2143A>T | ENSP00000512849.1:n.-148-2143A>T | |
ENST00000696751.1:c.364+391A>T | ENSP00000512850.1:n.364+391A>T | |
ENST00000231228.3:c.365-152A>T MANE Select | ENSP00000231228.2:n.365-152A>T | |
ENST00000231228.2:c.365-152A>T | ENSP00000231228.2:n.365-152A>T | |
NM_002187.2:c.365-152A>T , LRG_71t1:c.365-152A>T | NP_002178.2:n.365-152A>T | |
XR_001742945.1:n.147+2067T>A | ||
NM_002187.3:c.365-152A>T MANE Select | NP_002178.2:n.365-152A>T |